Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin–Lowry syndrome

Author: Zeniou Maria   Gattoni Renata   Hanauer André   Stévenin James  

Publisher: Oxford University Press

ISSN: 1362-4962

Source: Nucleic Acids Research, Vol.32, Iss.3, 2004-02, pp. : 1214-1223

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